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Gene : ROR2 Homo sapiens

Name  ? receptor tyrosine kinase like orphan receptor 2 Cytological Location  9q22.31
Brief Description  receptor tyrosine kinase like orphan receptor 2
Description  The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq, Jul 2008]
  • synonyms:
  • uc004arj.3,
  • OTTHUMG00000020211,
  • BDB,
  • NTRKR2,
  • HGNC:10257,
  • ROR2,
  • NTRKR2,
  • BDB1,
  • BDB1,
  • NM_001318204,
  • BDB,
  • M97639,
  • receptor tyrosine kinase-like orphan receptor 2
  • identifiers:
  • 4920,
  • ENSG00000169071,
  • ROR2

Genome feature

Region: gene ? Length: 227631  
Location: 9:91722598-91950228 reverse strand Cyto location: 9q22.31

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2 Diseases

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3756 SN Ps

5 Cross References

19 Data Sets

57 Homologues

0 Located Features

97 Rna Seq Results